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The Journal of Biological Chemistry|June 16, 2000
A human SCO2 mutation helps define the role of Sco1p in the cytochrome oxidase assembly pathwayE K Dickinson, D L Adams, E A Schon, et al.
Journal of the Neurological Sciences|September 1, 1991
Localization of mitochondrial DNA in normal and pathological muscle using immunological probes: a new approach to the study of mitochondrial myopathiesF Andreetta, H J Tritschler, E A Schon, et al.
Development (Cambridge, England)|June 18, 2021
Gene expression variation in Arabidopsis embryos at single-nucleus resolutionPing Kao, Michael A Schon, Magdalena Mosiolek, et al.
Journal of the American College of Nutrition|January 1, 1985
Total nutritional support through the peritoneal cavityR B Gilsdorf, R R Selby, D A Schon, et al.
American Journal of Human Genetics|October 23, 1997
The fate of human sperm-derived mtDNA in somatic cellsG Manfredi, D Thyagarajan, L C Papadopoulou, et al.
American Journal of Human Genetics|May 1, 1992
The mitochondrial tRNA(Leu(UUR)) mutation in mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes (MELAS): genetic, biochemical, and morphological correlations in skeletal muscleC T Moraes, E Ricci, E Bonilla, et al.
Molecular Biology of the Cell|November 14, 2002
An algal nucleus-encoded subunit of mitochondrial ATP synthase rescues a defect in the analogous human mitochondrial-encoded subunitJoseline Ojaimi, Junmin Pan, Sumana Santra, et al.
Nucleic Acids Research|October 24, 1980
Identification by nucleotide sequence analysis of a goat pseudoglobin geneM L Cleary, J R Haynes, E A Schon, et al.
The Journal of Biological Chemistry|October 25, 1987
Isolation of a cDNA encoding the muscle-specific subunit of human phosphoglycerate mutaseS Shanske, S Sakoda, M A Hermodson, et al.
Molecular and Cellular Biology|May 1, 1995
In vitro analysis of mutations causing myoclonus epilepsy with ragged-red fibers in the mitochondrial tRNA(Lys)gene: two genotypes produce similar phenotypesJ P Masucci, M Davidson, Y Koga, et al.
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